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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 15036289, 화합물 → HCID 15036290, 화합물

HRID 728580
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HRID 728580 반응식
[CH2:1]([C:3]([OH:18])([CH2:16][CH3:17])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([NH:10][C:11]([CH3:13])=[O:12])[C:5]=1[CH2:14][OH:15])[CH3:2]>O1CCCC1.[O-2].[O-2].[Mn+4]>[CH2:1]([C:3]1([CH2:16][CH3:17])[C:4]2[C:5](=[C:6]([NH:10][C:11]([CH3:13])=[O:12])[CH:7]=[CH:8][CH:9]=2)[C:14](=[O:15])[O:18]1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 15036289HCID 15036289, 화합물

생성물 1

HCID 15036290HCID 15036290, 화합물수율 62.2%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 8.0 g of α,α-diethyl-2-hydroxymethyl-3-acetaminobenzyl alcohol in 300 ml of tetrahydrofuran was added 32 g of activated manganese dioxide and the mixture was allowed to react for 6 hours under refluxing. After the reaction was over, the reaction mixture was left to stand for cooling and filtered on a glass filter having a bed of celite. The residue was washed with 100 ml of tetrahydrofuran. The filtrate and the washed solution were combined and concentrated to obtain an oily substance. The oily substance was purified by silica gel column chromatography to obtain 4.9 g of 3,3-diethyl-7-acetaminophthalide in the colorless oily substance.

후처리

  1. customto react for 6 hours
  2. temperatureunder refluxing
  3. waitwas left
  4. temperaturefor cooling
  5. filtrationfiltered on a glass
  6. filtrationfilter
  7. washThe residue was washed with 100 ml of tetrahydrofuran
  8. concentrationconcentrated
  9. customto obtain an oily substance
  10. customThe oily substance was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-bf1d55aca83741958100901949f36cb8
출처 데이터셋
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05049575

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